4.7 Article

Eszopiclone increases the respiratory arousal threshold and lowers the apnoea/hypopnoea index in obstructive sleep apnoea patients with a low arousal threshold

Journal

CLINICAL SCIENCE
Volume 120, Issue 11-12, Pages 505-514

Publisher

PORTLAND PRESS LTD
DOI: 10.1042/CS20100588

Keywords

apnoea/hypopnoae index (AHI); lung; sedative medication; sleep-disordered breathing; therapeutic target; upper-airway physiology

Funding

  1. National Institutes of Health (NIH) [P01 HL095491-01 A1, HL73146 R01 HL085188-01A2, R01 HL090897-01A2, K24 HL 093218-01 A1]
  2. Sepracor Pharmaceuticals
  3. National Health and Medical Research Council of Australia [510392]
  4. American Heart Association [10SDG3510018]
  5. Philips
  6. Medtronic
  7. Medtronic, Apnicure
  8. Medtronic, Apnicure, Apnex
  9. Itamar Ethicon
  10. Pfizer
  11. Separacor
  12. Merck
  13. Cephalon
  14. SGS
  15. SHC

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Recent insights into sleep apnoea pathogenesis reveal that a low respiratory arousal threshold (awaken easily) is important for many patients. As most patients experience stable breathing periods mediated by upper-airway dilator muscle activation via accumulation of respiratory stimuli, premature awakening may prevent respiratory stimuli build up as well as die resulting stabilization of sleep and breathing. The aim of the present physiological study was to determine the effects of a non-benzodiazepine sedative, eszopiclone, on the arousal threshold and the AHI (apnoea/hypopnoea index) in obstructive sleep apnoea patients. We hypothesized that eszopiclone would increase the arousal threshold and lower the AHI in patients with a low arousal threshold (0 to 15 cmH20). Following a baseline overnight polysomnogram with an epiglottic pressure catheter to quantify the arousal threshold, 17 obstructive sleep apnoea patients, without major hypoxaemia [nadir SaO(2) (arterial blood oxygen saturation) >70%], returned on two additional nights and received 3 mg of eszopiclone or placebo immediately prior to each study. Compared with placebo, eszopiclone significantly increased the arousal threshold [-14.0 (-19.9 to -10.9) compared with -18.0 (-22.2 to -15.1) cmH(2)O; P < 0.01], and sleep duration, improved sleep quality and lowered the AHI without respiratory event prolongation or worsening hypoxaemia. Among the eight patients identified as having a low arousal threshold, reductions in the AHI occurred invariably and were most pronounced (25 +/- 6 compared with 14 +/- 4 events/h of sleep; P < 0.01). In conclusion, eszopiclone increases the arousal threshold and lowers the AHI in obstructive sleep apnoea patients that do not have marked overnight hypoxa.emia. The greatest reductions in the AHI occurred in those with a low arousal threshold. The results of this single night physiological study suggest that certain sedatives may be of therapeutic benefit for a definable subgroup of patients. However, additional treatment strategies are probably required to achieve elimination of apnoea.

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